OMOP Concept 37161048
Combined oxidative phosphorylation defect type 25
StandardConditionSNOMED1173035001Disorder
Maps from
0
Descendants
0
Valid from
30 Sept 2021
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Combined oxidative phosphorylation defect type 25 across source vocabularies.
- Combined oxidative phosphorylation defect type 25 (disorder)
- COXPD25 - combined oxidative phosphorylation defect type 25
- defecto combinado de la fosforilación oxidativa tipo 25
- defecto combinado de la fosforilación oxidativa tipo 25 (trastorno)
- deficiencia combinada de la fosforilación oxidativa tipo 25
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Deficiency in enzyme complexes of mitochondrial respiratory chain
- 1Hereditary hearing loss
- 1Inherited metabolic disorder of nervous system
- 1Mitochondrial cytopathy
- 1Sensorineural hearing loss
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Disorder of mitochondrial respiratory chain complexes
- 2Enzymopathy
- 2Hearing loss
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Metabolic disease
- 3Congenital disease
- 3Disease
- 3Disorder of auditory system
- 3Disorder of nervous system
- 3Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 3Hearing disorder
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 4Clinical finding
- 4Disorder of body system
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